Variant DetailsVariant: dgv21n100Internal ID | 20151637 | Landmark | | Location Information | | Cytoband | 1p36.21 | Allele length | Assembly | Allele length | hg38 | 178660 | hg19 | 179628 | hg18 | 179628 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv998681, nsv998530, nsv1011809, nsv1010745, nsv1002288, nsv1006273, nsv997632, nsv1000920, nsv1006654 | Samples | | Known Genes | HNRNPCL1, LOC649330, PRAMEF1, PRAMEF10, PRAMEF11, PRAMEF12, PRAMEF2, PRAMEF4, PRAMEF6, PRAMEF7, PRAMEF8 | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | dgv21n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 72 | Observed Complex | 0 | Frequency | n/a |
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